A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3928967



Internal ID21349038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:56365905..56366003hg38UCSC Ensembl
chr20:54940961..54941059hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15179387
SamplesHG002
Known GenesFAM210B
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3928967
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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